ClinVar Miner

List of variants in gene SOS1 reported as likely benign

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 153
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HGVS dbSNP
NM_005633.3(SOS1):c.*12C>T rs1057522437
NM_005633.3(SOS1):c.*1333_*1336dupAAGT rs35969619
NM_005633.3(SOS1):c.*1606delT rs34248802
NM_005633.3(SOS1):c.*1731A>G rs79270739
NM_005633.3(SOS1):c.*1844A>G rs10166395
NM_005633.3(SOS1):c.*2244_*2245dupTA rs3832123
NM_005633.3(SOS1):c.*2439delA rs377250198
NM_005633.3(SOS1):c.*2567T>A rs6704656
NM_005633.3(SOS1):c.*328A>G rs1059310
NM_005633.3(SOS1):c.*3539T>C rs1037495
NM_005633.3(SOS1):c.*3592C>T rs550315455
NM_005633.3(SOS1):c.*3724T>C rs11124658
NM_005633.3(SOS1):c.*3918T>C rs1043793
NM_005633.3(SOS1):c.*399_*400insCA rs144104838
NM_005633.3(SOS1):c.*805C>A rs1059313
NM_005633.3(SOS1):c.*8T>C rs1057521160
NM_005633.3(SOS1):c.-21C>G rs1057520420
NM_005633.3(SOS1):c.-32C>T rs1057520479
NM_005633.3(SOS1):c.-43C>T rs1016843875
NM_005633.3(SOS1):c.1018C>T (p.Pro340Ser) rs190222208
NM_005633.3(SOS1):c.1074+126C>T
NM_005633.3(SOS1):c.1074+5G>C rs145155424
NM_005633.3(SOS1):c.109A>G (p.Thr37Ala) rs150565592
NM_005633.3(SOS1):c.115G>A (p.Glu39Lys)
NM_005633.3(SOS1):c.1191A>G (p.Lys397=) rs770175415
NM_005633.3(SOS1):c.1202+5A>G rs1021449471
NM_005633.3(SOS1):c.1203-13T>A rs145166996
NM_005633.3(SOS1):c.1203-17C>G rs1553356202
NM_005633.3(SOS1):c.1203-22_1203-20dupAAT rs1553356212
NM_005633.3(SOS1):c.1203-41C>T rs568590951
NM_005633.3(SOS1):c.1230G>A (p.Gln410=) rs141390073
NM_005633.3(SOS1):c.1269C>T (p.Asn423=) rs138459502
NM_005633.3(SOS1):c.1428G>A (p.Gly476=)
NM_005633.3(SOS1):c.1434A>T (p.Pro478=) rs368495902
NM_005633.3(SOS1):c.1458A>G (p.Ala486=) rs772746896
NM_005633.3(SOS1):c.1489C>A (p.Arg497=) rs542368621
NM_005633.3(SOS1):c.1491A>G (p.Arg497=) rs1432437086
NM_005633.3(SOS1):c.1621T>C (p.Leu541=) rs371286473
NM_005633.3(SOS1):c.162A>G (p.Gln54=) rs763520126
NM_005633.3(SOS1):c.1647A>G (p.Thr549=) rs139683425
NM_005633.3(SOS1):c.1648C>T (p.Leu550=) rs1233000238
NM_005633.3(SOS1):c.1705C>G (p.Leu569Val) rs200786705
NM_005633.3(SOS1):c.1707G>A (p.Leu569=) rs1479407572
NM_005633.3(SOS1):c.1719T>C (p.Asp573=) rs746674452
NM_005633.3(SOS1):c.1770G>A (p.Glu590=) rs553331572
NM_005633.3(SOS1):c.1842G>A (p.Thr614=) rs143750479
NM_005633.3(SOS1):c.1848T>C (p.His616=) rs1344852617
NM_005633.3(SOS1):c.1854C>T (p.Tyr618=) rs727505181
NM_005633.3(SOS1):c.1859-5_1859-3delCTT rs1171459346
NM_005633.3(SOS1):c.1863C>T (p.Pro621=) rs759125551
NM_005633.3(SOS1):c.1940+34T>C
NM_005633.3(SOS1):c.1953A>G (p.Pro651=) rs141507912
NM_005633.3(SOS1):c.195A>C (p.Arg65=) rs7609455
NM_005633.3(SOS1):c.1962G>A (p.Glu654=) rs144382701
NM_005633.3(SOS1):c.1987A>G (p.Ile663Val) rs730881024
NM_005633.3(SOS1):c.2061G>A (p.Leu687=) rs727504752
NM_005633.3(SOS1):c.2063+44T>C rs111576630
NM_005633.3(SOS1):c.2064-20A>T rs756707478
NM_005633.3(SOS1):c.2122G>A (p.Ala708Thr) rs140811086
NM_005633.3(SOS1):c.213+14_213+16delTGT rs768872084
NM_005633.3(SOS1):c.213+16T>C rs150536159
NM_005633.3(SOS1):c.214-10A>G rs371447614
NM_005633.3(SOS1):c.2156G>C (p.Gly719Ala) rs200794965
NM_005633.3(SOS1):c.2167+6T>G rs186640807
NM_005633.3(SOS1):c.2168-42_2168-39delTAAA
NM_005633.3(SOS1):c.2168-50A>C rs778705378
NM_005633.3(SOS1):c.21C>T (p.Pro7=) rs727504845
NM_005633.3(SOS1):c.2238T>C (p.Asn746=) rs75877625
NM_005633.3(SOS1):c.225A>G (p.Gln75=) rs560037748
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2510+19C>G rs375675348
NM_005633.3(SOS1):c.2511-13_2511-9delTTTTT rs727503436
NM_005633.3(SOS1):c.2511-98C>G
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.3(SOS1):c.2673+14T>C rs183998234
NM_005633.3(SOS1):c.2674-22C>G rs61601281
NM_005633.3(SOS1):c.2674-9dup rs532594344
NM_005633.3(SOS1):c.2728G>C (p.Asp910His) rs369277679
NM_005633.3(SOS1):c.2739G>A (p.Lys913=) rs997339872
NM_005633.3(SOS1):c.273A>G (p.Gln91=) rs914110575
NM_005633.3(SOS1):c.2760G>A (p.Arg920=) rs149092581
NM_005633.3(SOS1):c.2775A>T (p.Pro925=) rs397517160
NM_005633.3(SOS1):c.2791+11C>G rs1057521862
NM_005633.3(SOS1):c.2791+7_2791+10delATTT rs760707217
NM_005633.3(SOS1):c.2792-48T>C rs540132304
NM_005633.3(SOS1):c.2792-71C>T
NM_005633.3(SOS1):c.280A>G (p.Ile94Val) rs144757941
NM_005633.3(SOS1):c.2838G>A (p.Glu946=) rs397517162
NM_005633.3(SOS1):c.2868A>C (p.Ile956=) rs758834690
NM_005633.3(SOS1):c.294G>A (p.Lys98=) rs748478952
NM_005633.3(SOS1):c.2966G>A (p.Arg989Lys) rs202043599
NM_005633.3(SOS1):c.2997T>C (p.Asn999=) rs145364368
NM_005633.3(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934
NM_005633.3(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671
NM_005633.3(SOS1):c.3060C>T (p.Asn1020=) rs142431345
NM_005633.3(SOS1):c.3072C>T (p.Leu1024=) rs558386297
NM_005633.3(SOS1):c.3082-331C>G
NM_005633.3(SOS1):c.3189T>C (p.Ile1063=)
NM_005633.3(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034
NM_005633.3(SOS1):c.3303T>C (p.Val1101=) rs397517165
NM_005633.3(SOS1):c.3330G>C (p.Ser1110=) rs146383828
NM_005633.3(SOS1):c.3350A>G (p.Asn1117Ser) rs754314057
NM_005633.3(SOS1):c.3357C>T (p.Thr1119=) rs373319212
NM_005633.3(SOS1):c.3369A>G (p.Gln1123=) rs727503435
NM_005633.3(SOS1):c.3384T>C (p.His1128=)
NM_005633.3(SOS1):c.3391+7A>G rs201982464
NM_005633.3(SOS1):c.345+12_345+13dupCT rs397517167
NM_005633.3(SOS1):c.350T>G (p.Val117Gly) rs201085754
NM_005633.3(SOS1):c.3511-14_3511-10delTTTTC rs760713912
NM_005633.3(SOS1):c.3511-18A>T
NM_005633.3(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736
NM_005633.3(SOS1):c.3600C>T (p.Asp1200=) rs141594736
NM_005633.3(SOS1):c.3601C>T (p.Arg1201Trp)
NM_005633.3(SOS1):c.3620C>G (p.Pro1207Arg) rs730881025
NM_005633.3(SOS1):c.3658G>A (p.Val1220Met) rs776814547
NM_005633.3(SOS1):c.3703C>T (p.Pro1235Ser) rs397517168
NM_005633.3(SOS1):c.3706C>A (p.Pro1236Thr) rs727504636
NM_005633.3(SOS1):c.3709C>A (p.Pro1237Thr) rs371408734
NM_005633.3(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026
NM_005633.3(SOS1):c.3801C>T (p.His1267=) rs747676700
NM_005633.3(SOS1):c.3802G>A (p.Gly1268Ser) rs730881051
NM_005633.3(SOS1):c.3813G>A (p.Arg1271=) rs863224405
NM_005633.3(SOS1):c.3859A>G (p.Ile1287Val) rs760917490
NM_005633.3(SOS1):c.3900A>G (p.Gln1300=) rs1343754754
NM_005633.3(SOS1):c.3948C>T (p.His1316=) rs1399242305
NM_005633.3(SOS1):c.396A>T (p.Ala132=) rs727505385
NM_005633.3(SOS1):c.3996T>C (p.Ser1332=) rs1057522315
NM_005633.3(SOS1):c.39A>G (p.Glu13=) rs763337946
NM_005633.3(SOS1):c.511-9_511-6delACTG rs986512473
NM_005633.3(SOS1):c.543A>G (p.Glu181=) rs201068374
NM_005633.3(SOS1):c.552T>C (p.Asn184=) rs727503438
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.582C>T (p.Ser194=) rs746685895
NM_005633.3(SOS1):c.588A>T (p.Ser196=) rs727504826
NM_005633.3(SOS1):c.597A>G (p.Gln199=) rs397517175
NM_005633.3(SOS1):c.643T>C (p.Tyr215His) rs730881039
NM_005633.3(SOS1):c.675T>G (p.Val225=) rs371482290
NM_005633.3(SOS1):c.688T>G (p.Phe230Val) rs397517177
NM_005633.3(SOS1):c.698A>G (p.Asn233Ser) rs144934321
NM_005633.3(SOS1):c.720+9C>T rs370687707
NM_005633.3(SOS1):c.73C>T (p.Pro25Ser) rs139592595
NM_005633.3(SOS1):c.749T>C (p.Val250Ala) rs139290271
NM_005633.3(SOS1):c.798A>C (p.Thr266=) rs756044708
NM_005633.3(SOS1):c.822T>C (p.Ser274=) rs1057522964
NM_005633.3(SOS1):c.864+12A>C
NM_005633.3(SOS1):c.865-344A>T
NM_005633.3(SOS1):c.865-49G>A
NM_005633.3(SOS1):c.87+12G>T rs368569135
NM_005633.3(SOS1):c.87+88delG
NM_005633.3(SOS1):c.87+9C>T rs397517179
NM_005633.3(SOS1):c.88-7T>A rs1416502603
NM_005633.3(SOS1):c.899G>A (p.Arg300Gln) rs754374236
NM_005633.3(SOS1):c.976-5dupT rs771586560

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